Modulation of Broiler Intestinal Changes Induced by Clostridium perfringens and Deoxynivalenol through Probiotic, Paraprobiotic, and Postbiotic Supplementation.

Deoxynivalenol (DON) is a predisposing factor for necrotic enteritis. This study aimed to investigate the effects of a DON and Clostridium perfringens (CP) challenge on the intestinal morphology, morphometry, oxidative stress, and immune response of broilers. Additionally, we evaluated the potential of a Lactobacillus spp. mixture as an approach to mitigate the damage induced by the challenge. One-day-old broiler chickens (n = 252) were divided into seven treatment groups: Control, DON, CP, CP + DON, VL (DON + CP + viable Lactobacillus spp. mixture), HIL (DON + CP + heat-inactivated Lactobacillus spp. mixture), and LCS (DON + CP + Lactobacillus spp. mixture culture supernatant). Macroscopic evaluation of the intestines revealed that the CP + DON group exhibited the highest lesion score, while the VL and HIL groups showed the lowest scores. Microscopically, all Lactobacillus spp. treatments mitigated the morphological changes induced by the challenge. DON increased levels of reactive oxygen species (ROS) in the jejunum, and CP increased ROS levels in the jejunum and ileum. Notably, the Lactobacillus spp. treatments did not improve the antioxidant defense against CP-induced oxidative stress. In summary, a Lactobacillus spp. mixture, whether used as a probiotic, paraprobiotic, or postbiotic, exerted a partially protective effect in mitigating most of the intestinal damage induced by DON and CP challenges.

Resistance and Virulence Surveillance in Escherichia coli Isolated from Commercial Meat Samples: A One Health Approach.

Escherichia coli is a key indicator of food hygiene, and its monitoring in meat samples points to the potential presence of antimicrobial-resistant strains capable of causing infections in humans, encompassing resistance profiles categorized as serious threats by the Centers for Disease Control and Prevention (CDC), such as Extended-Spectrum Beta-Lactamase (ESBL)-a problem with consequences for animal, human, and environmental health. The objective of the present work was to isolate and characterize ESBL-producing E. coli strains from poultry, pork, and beef meat samples, with a characterization of their virulence and antimicrobial resistance profiles. A total of 450 meat samples (150 chicken, 150 beef, and 150 pork) were obtained from supermarkets and subsequently cultured in medium supplemented with cefotaxime. The isolated colonies were characterized biochemically, followed by antibiogram testing using the disk diffusion technique. Further classification involved biofilm formation and the presence of antimicrobial resistance genes (blaCTX-M, AmpC-type, mcr-1, and fosA3), and virulence genes (eaeA, st, bfpA, lt, stx1, stx2, aggR, iss, ompT, hlyF, iutA, iroN, fyuA, cvaC, and hylA). Statistical analysis was performed via the likelihood-ratio test. In total, 168 strains were obtained, with 73% originating from chicken, 22% from pork, and 17% from beef samples. Notably, strains exhibited greater resistance to tetracycline (51%), ciprofloxacin (46%), and fosfomycin (38%), apart from ß-lactams. The detection of antimicrobial resistance in food-isolated strains is noteworthy, underscoring the significance of antimicrobial resistance as a global concern. More than 90% of the strains were biofilm producers, and strains carrying many ExPEC genes were more likely to be biofilm formers (OR 2.42), which increases the problem since the microorganisms have a greater chance of environment persistence and genetic exchange. Regarding molecular characterization, bovine samples showed a higher prevalence of blaCTX-M-1 (OR 6.52), while chicken strains were more likely to carry the fosA3 gene (OR 2.43, CI 1.17-5.05) and presented between 6 to 8 ExPEC genes (OR 2.5, CI 1.33-5.01) compared to other meat samples. Concerning diarrheagenic E. coli genes, two strains harbored eae. It is important to highlight these strains, as they exhibited both biofilm-forming capacities and multidrug resistance (MDR), potentially enabling colonization in diverse environments and causing infections. In conclusion, this study underscores the presence of ß-lactamase-producing E. coli strains, mainly in poultry samples, compared to beef and pork samples. Furthermore, all meat sample strains exhibited many virulence-associated extraintestinal genes, with some strains harboring diarrheagenic E. coli (DEC) genes.

Prevalence of Antimicrobial Resistance and Clonal Relationship in ESBL/AmpC-Producing Proteus mirabilis Isolated from Meat Products and Community-Acquired Urinary Tract Infection (UTI-CA) in Southern Brazil.

The present study aimed to evaluate the prevalence of antimicrobial resistance and clonal relationships in Proteus mirabilis isolated from chicken meat, beef, pork, and community-acquired urinary tract infections (UTI-CA). Chicken meat isolates showed the highest multidrug resistance (MDR), followed by those from pork and UTI-CA, whereas beef had relatively few MDR strains. All sources had strains that carried blaCTX-M-65, whereas blaCTX-M-2 and blaCMY-2 were only detected in chicken meat and UTI-CA isolates. This indicates that chicken meat should be considered an important risk factor for the spread of P. mirabilis carrying ESBL and AmpC. Furthermore, ESBL/AmpC producing strains were resistant to a greater number of antimicrobials and possessed more resistance genes than non-producing strains. In addition, the antimicrobial resistance genes qnrD, aac(6')-Ib-cr, sul1, sul2, fosA3, cmlA, and floR were also found. Molecular typing showed a genetic similarity between chicken meat and UTI-CA isolates, including some strains with 100% similarity, indicating that chicken can be a source of P. mirabilis causing UTI-CA. It was concluded that meat, especially chicken meat, can be an important source of dissemination of multidrug-resistant P. mirabilis in the community.

High-Frequency Detection of fosA3 and bla CTX-M-55 Genes in Escherichia coli From Longitudinal Monitoring in Broiler Chicken Farms.

Considering the worrying emergence of multidrug resistance, including in animal husbandry and especially in food-producing animals, the need to detect antimicrobial resistance strains in poultry environments is relevant, mainly considering a One Health approach. Thus, this study aimed to conduct longitudinal monitoring of antimicrobial resistance in broiler chicken farms, with an emphasis on evaluating the frequency of resistance to fosfomycin and ß-lactams. Escherichia coli was isolated from broiler chicken farms (cloacal swabs, meconium, poultry feed, water, poultry litter, and Alphitobius diaperinus) in northern Paraná from 2019 to 2020 during three periods: the first period (1st days of life), the second period (20th to 25th days of life), and third period (40th to 42nd days of life). Antibiogram tests and the detection of phenotypic extended-spectrum ß-lactamase (ESBL) were performed, and they were confirmed by seaching for genes from the bla CTX-M group. The other resistance genes searched were mcr-1 and fosA3. Some ESBL bla CTX-M-1 group strains were selected for ESBL identification by sequencing and enterobacterial repetitive intergenic consensus-polymerase chain reaction analysis. To determine the transferability of the bla CTX-M-1- and fosA3-carrying plasmids, strains were subjected to conjugation experiments. A total of 507 E. coli were analyzed: 360 from cloacal swabs, 24 from meconium samples, 3 from poultry feed samples, 18 from water samples, 69 from poultry litter samples, and 33 from A. diaperinus samples. Among the strain isolate, 80% (406/507) were multidrug-resistant (MDR), and 51% (260/507) were ESBL-positive, with the bla CTX-M-1 group being the most frequent. For the fosA3 gene, 68% (344/507) of the strains isolated were positive, deserves to be highlighted E. coli isolated from day-old chickens (OR 6.34, CI 2.34-17.17), when compared with strains isolated from other origins (poultry litter, A. diaperinus, water, and poultry feed). This work alerts us to the high frequency of the fosA3 gene correlated with the CTX-M-1 group (OR 3.57, CI 95% 2.7-4.72, p < 0.05), especially the bla CTX-M-55 gene, in broiler chickens. This profile was observed mainly in day-old chicken, with a high percentage of E. coli that were MDR. The findings emphasize the importance of conducting longitudinal monitoring to detect the primary risk points during poultry production.

Histological evaluation of the intestine of broiler chickens: comparison of three sampling methods / Avaliação histológica do intestino de frangos de corte: comparação de três métodos de colheita

After the growth-promoting antibiotics prohibition, intestinal health became an increasing concern worldwide in poultry farming. The intestinal histological evaluation is an inexpensive technique that brings relevant information, but in poultry, the immediate process of intestinal post-mortem autolysis interferes directly on the samples quality for histological analysis hindering a precise diagnosis. This study aimed to standardize a technique for broilers' intestines sample collection and fixation for histological analysis. Seven broiler chickens received a standard diet until 23 days of age when they were euthanized. Fragments of duodenum, jejunum, and ileum were collected using three methods: intestine strips, transverse section, and Swiss roll and posteriorly fixed in 10% buffered formalin and bouin solution. Tissue samples were submitted for histological (number of villi and viable villi per field) and morphometrical (villi height, cryptdepth and villi:crypt ratio) evaluations and the results analyzed statistically. A significant high number of villiand viable villi per field in all regions was observed in the Swiss roll method. In the duodenum (p= 0.0066) and jejunum (p= 0.0058) an interaction between the Swiss roll method and the fixative buffered formalin was observed in the viable and number of villi per field, respectively. Regarding the morphometrical analysis significant differences were observed, in the jejunum villi height sampling by the methods Swissroll (1,157.66 ± 148.25 µm, p= 0.0015) that showed the highest mean. Deeper crypt depths were observed in the jejunum (156.59 ± 15.68 µm, p= 0.0002) and ileum (131.13 ± 15.01 µm, p= 0.0006) collect by the Swissroll method. An interaction between the bouin fixative was also observed in the [...].

Após a proibição da utilização dos antimicrobianos promotores de crescimento, saúde intestinal se tornou uma preocupação crescente na avicultura mundialmente. A avaliação histológica intestinal é uma técnica de baixo custo que traz informações relevantes, porém nas aves, o imediato processo de autólise intestinal post-mortem interfere diretamente na qualidade da amostra para histologia dificultando um diagnóstico preciso. Este estudo objetivou a padronização de uma técnica para coleta e fixação do intestino de frangos de corte para análise histológica. Sete frangos de corte receberam uma dieta padrão até 23 dias de vida, quando foram eutanasiados. Fragmentos de duodeno, jejuno e íleo foram coletados utilizando três métodos: intestino aberto, corte transversal e rocambole, e posteriormente fixados em formalina tamponada10% e solução de bouin. Amostras de tecidos foram submetidas a avaliações histológicas (número de vilosidades e vilosidades viáveis por campo) e morfométricas (altura de vilosidade, profundidade de cripta e relação vilosidade:cripta) e os resultados analisados estatisticamente. Um significativo maior número de vilosidades e vilosidades viáveis por campo foi observado, em todos os segmentos intestinais, no método rocambole. No duodeno (p= 0,0066) e jejuno (p= 0,0058) uma interação entre o método rocambole e o fixador formalina tamponada foi observado para as variáveis vilosidades viáveis e número de vilosidades por campo, respectivamente. Referente a análise morfométrica diferenças significativas foram observadas na altura de vilosidade no jejuno amostrado pelo método rocambole (1.157,66 ± 148,25 µm, p= 0,0015)que apresentou a maior média. Criptas mais profundas foram observadas no jejuno (156,59 ± 15,68 µm, p= 0,0002) e íleo (131,13 ± 15,01 µm, p= 0,0006) coletados pelo método rocambole. Uma interação entre o fixador bouin também foi observado no jejuno (p= 0,0223) para esta variável. Amostragem do [...]

Histological evaluation of the intestine of broiler chickens: comparison of three sampling methods / Avaliação histológica do intestino de frangos de corte: comparação de três métodos de colheita

After the growth-promoting antibiotics prohibition, intestinal health became an increasing concern worldwide in poultry farming. The intestinal histological evaluation is an inexpensive technique that brings relevant information, but in poultry, the immediate process of intestinal post-mortem autolysis interferes directly on the samples quality for histological analysis hindering a precise diagnosis. This study aimed to standardize a technique for broilers' intestines sample collection and fixation for histological analysis. Seven broiler chickens received a standard diet until 23 days of age when they were euthanized. Fragments of duodenum, jejunum, and ileum were collected using three methods: intestine strips, transverse section, and Swiss roll and posteriorly fixed in 10% buffered formalin and bouin solution. Tissue samples were submitted for histological (number of villi and viable villi per field) and morphometrical (villi height, cryptdepth and villi:crypt ratio) evaluations and the results analyzed statistically. A significant high number of villiand viable villi per field in all regions was observed in the Swiss roll method. In the duodenum (p= 0.0066) and jejunum (p= 0.0058) an interaction between the Swiss roll method and the fixative buffered formalin was observed in the viable and number of villi per field, respectively. Regarding the morphometrical analysis significant differences were observed, in the jejunum villi height sampling by the methods Swissroll (1,157.66 ± 148.25 µm, p= 0.0015) that showed the highest mean. Deeper crypt depths were observed in the jejunum (156.59 ± 15.68 µm, p= 0.0002) and ileum (131.13 ± 15.01 µm, p= 0.0006) collect by the Swissroll method. An interaction between the bouin fixative was also observed in the [...].(AU)

Após a proibição da utilização dos antimicrobianos promotores de crescimento, saúde intestinal se tornou uma preocupação crescente na avicultura mundialmente. A avaliação histológica intestinal é uma técnica de baixo custo que traz informações relevantes, porém nas aves, o imediato processo de autólise intestinal post-mortem interfere diretamente na qualidade da amostra para histologia dificultando um diagnóstico preciso. Este estudo objetivou a padronização de uma técnica para coleta e fixação do intestino de frangos de corte para análise histológica. Sete frangos de corte receberam uma dieta padrão até 23 dias de vida, quando foram eutanasiados. Fragmentos de duodeno, jejuno e íleo foram coletados utilizando três métodos: intestino aberto, corte transversal e rocambole, e posteriormente fixados em formalina tamponada10% e solução de bouin. Amostras de tecidos foram submetidas a avaliações histológicas (número de vilosidades e vilosidades viáveis por campo) e morfométricas (altura de vilosidade, profundidade de cripta e relação vilosidade:cripta) e os resultados analisados estatisticamente. Um significativo maior número de vilosidades e vilosidades viáveis por campo foi observado, em todos os segmentos intestinais, no método rocambole. No duodeno (p= 0,0066) e jejuno (p= 0,0058) uma interação entre o método rocambole e o fixador formalina tamponada foi observado para as variáveis vilosidades viáveis e número de vilosidades por campo, respectivamente. Referente a análise morfométrica diferenças significativas foram observadas na altura de vilosidade no jejuno amostrado pelo método rocambole (1.157,66 ± 148,25 µm, p= 0,0015)que apresentou a maior média. Criptas mais profundas foram observadas no jejuno (156,59 ± 15,68 µm, p= 0,0002) e íleo (131,13 ± 15,01 µm, p= 0,0006) coletados pelo método rocambole. Uma interação entre o fixador bouin também foi observado no jejuno (p= 0,0223) para esta variável. Amostragem do [...](AU)

Peritonitis and necrotizing hepatitis in Ara ararauna caused by a foreign body

Background: The ingestion of foreign bodies in parrots has already been described and associated with the curious behaviorof the birds or with stressful conditions. Foreign bodies in the gastrointestinal tract are usually diagnosed through clinicalsigns, laboratory tests, and radiographic findings in the historical data. Foreign bodies are usually metallic and can lodgein any segment of the gastrointestinal tract, commonly found in the proventricle and gizzard. This study investigated acase of necrotizing hepatitis due to a foreign body in Ara ararauna (Linnaeus, 1758).Case: An approximately 9-month-old specimen of caninde macaw, had sudden death and was referred for autopsy. Themacroscopic examination revealed a fibrous, thick, reddish membrane involving the left hepatic lobe and partially the gizzard in continuity with the peritoneum. Inside the capsule, the liver had a friable and necrotic appearance and the gizzardhad a focal perforation area containing a foreign body (gavage tube feeding). We performed the histopathological examination of the liver and gizzard and observed that the membrane surrounding the liver and partially the gizzard had a chronicinflammatory process with a marked proliferation of fibrous tissue and fibrin deposition. The hepatic parenchyma of theleft lobe showed diffuse and marked necrosis, with signs of ischemic necrosis. In the region of transmural perforation ofthe gizzard, the mucosa showed a focal area of extensive necrosis accompanied by the presence of intralesional bacteria.The lesions observed are attributed to the perforation of the organs by the foreign body. It is not known whether the birdingested the object accidently during food handling as a young or due to the curious behavior of the bird or even the stressit may have been exposed to. The post mortem examination revealed localized peritonitis...(AU)

Peritonitis and necrotizing hepatitis in Ara ararauna caused by a foreign body

Background: The ingestion of foreign bodies in parrots has already been described and associated with the curious behaviorof the birds or with stressful conditions. Foreign bodies in the gastrointestinal tract are usually diagnosed through clinicalsigns, laboratory tests, and radiographic findings in the historical data. Foreign bodies are usually metallic and can lodgein any segment of the gastrointestinal tract, commonly found in the proventricle and gizzard. This study investigated acase of necrotizing hepatitis due to a foreign body in Ara ararauna (Linnaeus, 1758).Case: An approximately 9-month-old specimen of caninde macaw, had sudden death and was referred for autopsy. Themacroscopic examination revealed a fibrous, thick, reddish membrane involving the left hepatic lobe and partially the gizzard in continuity with the peritoneum. Inside the capsule, the liver had a friable and necrotic appearance and the gizzardhad a focal perforation area containing a foreign body (gavage tube feeding). We performed the histopathological examination of the liver and gizzard and observed that the membrane surrounding the liver and partially the gizzard had a chronicinflammatory process with a marked proliferation of fibrous tissue and fibrin deposition. The hepatic parenchyma of theleft lobe showed diffuse and marked necrosis, with signs of ischemic necrosis. In the region of transmural perforation ofthe gizzard, the mucosa showed a focal area of extensive necrosis accompanied by the presence of intralesional bacteria.The lesions observed are attributed to the perforation of the organs by the foreign body. It is not known whether the birdingested the object accidently during food handling as a young or due to the curious behavior of the bird or even the stressit may have been exposed to. The post mortem examination revealed localized peritonitis...

Histological evaluation of the intestine of broiler chickens: comparison of three sampling methods / Avaliação histológica do intestino de frangos de corte: comparação de três métodos de colheita

After the growth-promoting antibiotics prohibition, intestinal health became an increasing concern worldwide in poultry farming. The intestinal histological evaluation is an inexpensive technique that brings relevant information, but in poultry, the immediate process of intestinal post-mortem autolysis interferes directly on the samples quality for histological analysis hindering a precise diagnosis. This study aimed to standardize a technique for broilers' intestines sample collection and fixation for histological analysis. Seven broiler chickens received a standard diet until 23 days of age when they were euthanized. Fragments of duodenum, jejunum, and ileum were collected using three methods: intestine strips, transverse section, and Swiss roll and posteriorly fixed in 10% buffered formalin and bouin solution. Tissue samples were submitted for histological (number of villi and viable villi per field) and morphometrical (villi height, crypt depth and villi:crypt ratio) evaluations and the results analyzed statistically. A significant high number of villi and viable villi per field in all regions was observed in the Swiss roll method. In the duodenum (p= 0.0066) and jejunum (p= 0.0058) an interaction between the Swiss roll method and the fixative buffered formalin was observed in the viable and number of villi per field, respectively. Regarding the morphometrical analysis significant differences were observed, in the jejunum villi height sampling by the methods Swiss roll (1,157.66 ± 148.25 µm, p= 0.0015) that showed the highest mean. Deeper crypt depths were observed in the jejunum (156.59 ± 15.68 µm, p= 0.0002) and ileum (131.13 ± 15.01 µm, p= 0.0006) collect by the Swiss roll method. An interaction between the bouin fixative was also observed in the jejunum (p= 0.0223) for this variable. Duodenum sampling by transversal section (12.68 ± 1.45 µm, p= 0.0076) was the only segment that had a significant difference for villi:crypt ratio, showing the highest mean. It can be concluded that the Swiss roll technique was the best method for morphometrical evaluation of the chickens' intestines, since the highest counts of villi per field and viable villi per field were obtained, while buffered formalin was considered as the best fixative.(AU)

Após a proibição da utilização dos antimicrobianos promotores de crescimento, saúde intestinal se tornou uma preocupação crescente na avicultura mundialmente. A avaliação histológica intestinal é uma técnica de baixo custo que traz informações relevantes, porém nas aves, o imediato processo de autólise intestinal post-mortem interfere diretamente na qualidade da amostra para histologia dificultando um diagnóstico preciso. Este estudo objetivou a padronização de uma técnica para coleta e fixação do intestino de frangos de corte para análise histológica. Sete frangos de corte receberam uma dieta padrão até 23 dias de vida, quando foram eutanasiados. Fragmentos de duodeno, jejuno e íleo foram coletados utilizando três métodos: intestino aberto, corte transversal e rocambole, e posteriormente fixados em formalina tamponada 10% e solução de bouin. Amostras de tecidos foram submetidas a avaliações histológicas (número de vilosidades e vilosidades viáveis por campo) e morfométricas (altura de vilosidade, profundidade de cripta e relação vilosidade:cripta) e os resultados analisados estatisticamente. Um significativo maior número de vilosidades e vilosidades viáveis por campo foi observado, em todos os segmentos intestinais, no método rocambole. No duodeno (p= 0,0066) e jejuno (p= 0,0058) uma interação entre o método rocambole e o fixador formalina tamponada foi observado para as variáveis vilosidades viáveis e número de vilosidades por campo, respectivamente. Referente a análise morfométrica diferenças significativas foram observadas na altura de vilosidade no jejuno amostrado pelo método rocambole (1.157,66 ± 148,25 µm, p= 0,0015) que apresentou a maior média. Criptas mais profundas foram observadas no jejuno (156,59 ± 15,68 µm, p= 0,0002) e íleo (131,13 ± 15,01 µm, p= 0,0006) coletados pelo método rocambole. Uma interação entre o fixador bouin também foi observado no jejuno (p= 0,0223) para esta variável. Amostragem do duodeno pelo método corte transversal (12,68 ± 1,45 µm, p= 0,0076) foi o único segmento que teve uma diferença significativa para relação vilosidade:cripta apresentando a maior média. Pode-se concluir que o método rocambole foi o melhor para avaliação morfométrica do intestino de frangos de corte, uma vez que as maiores contagens de vilosidades e vilosidades viáveis por campo foram obtidas, enquanto formalina tamponada foi considerada o melhor fixador.(AU)

Proteus mirabilis causing cellulitis in broiler chickens.

Given the need to understand the virulence profile of Proteus mirabilis isolates from cellulitis in broiler chickens and their ability to cause lesions, the present study aimed to characterize genotypically and phenotypically the virulence profiles of two strains of P. mirabilis isolated from cellulitis in broilers, as well as to evaluate their ability to experimentally reproduce the lesions in vivo. The strain with the highest virulence potential (LBUEL-A33) possessed mrpA, pmfA, ucaA, atfA (fimbriae), zapA, ptA (proteases), hpmA (hemolysin), and ireA (siderophore) genes, formed a very strong biofilm, and expressed the pattern of aggregative adhesion and cytotoxicity in Vero cells. The strain with the lowest virulence potential (LBUEL-A34) did not present the pmfA and ucaA genes, but expressed the pattern of aggregative adhesion, formed a strong biofilm, and did not show cytotoxicity. Both strains developed cellulitis in an animal model within 24 h post-inoculation (PI), and the degree of lesions was not significantly altered up to 120 h PI. The LBUEL-A33 strain was also inoculated in combination with an avian pathogenic Escherichia coli (APEC 046), and the lesions showed no significant changes from the individual inoculation of these two strains. Histological analysis showed that the LBUEL-A33 strain developed characteristic cellulitis lesions. Thus, both strains of P. mirabilis isolated in our study have several virulence factors and the ability to develop cellulitis in broilers.

Genotypic and phenotypic profiles of virulence factors and antimicrobial resistance of Proteus mirabilis isolated from chicken carcasses: potential zoonotic risk.

Proteus mirabilis is an opportunistic pathogen often associated with a variety of human infections acquired both in the community and in hospitals. In this context, the present work aimed to evaluate the genotypic and phenotypic characteristics of the virulence factors and antimicrobial resistance determinants of 32 P. mirabilis strains isolated from chicken carcasses in a poultry slaughterhouse in the north of the state of Paraná, Brazil, in order to assess a potential zoonotic risk. The isolates presented a variety of virulence genes that contribute to the development of infection in humans. The mrpA, pmfA, atfA (fimbriae), ireA (siderophores receptor), zapA, ptA (Proteases), and hpmA (hemolysin) genes were found in 32 (100%) isolates and ucaA (fimbriae) in 16 (50%). All isolates showed aggregative adherence in HEp-2 cells and formed biofilms. Of all strains, 27 (84.38%) showed cytotoxic effects in Vero cells. Antimicrobial susceptibility was tested using 20 antimicrobials, in which 25 (78.13%) strains were considered multidrug-resistant. The presence of blaESBL and blaampC genes conferring resistance to ß-lactams and qnr to quinolones were also detected in the isolates after presumption in the phenotypic test, in which 7 (21.88%) isolates contained the CTX-M-2 group, 11 (34.38%) contained CIT group and 19 (59.38%) contained qnrD. Therefore, chicken carcasses contaminated with P. mirabilis may pose a health risk to the consumer, as these isolates have a variety of virulence and antimicrobial resistance characteristics that can be found in P. mirabilis strains isolated from human infections.

Multidrug resistant and ESBL-producing Salmonella spp. isolated from poultry / Salmonella spp. produtora de ESBL e multirresistente a drogas isolada de frangos

Salmonella spp. is one of the main agents responsible for foodborne infection in humans, and products of poultry origin are the most common infection sources. Studies have shown the occurrence of antimicrobials resistant Salmonella spp. in animal products. The Extended Spectrum β-Lactamase (ESBL) are enzymes that confer to bacteria the ability to hydrolyze cephalosporin with an oximino side chain and monobactams. This study aimed to investigate antimicrobial resistance profile, identify phenotypes and genotypes for multiple drug resistance (MDR) and that produce ESBL from isolates of Salmonella spp. in the broiler production chain. We used samples of Salmonella spp. (n=11) isolates from poultry, poultry products and poultry-source environment from the state of Maranhão - Brazil. The isolates of Salmonella spp. assessed showed genotypical and phenotypical characteristics of MDR. The results show that 72.72% (08/11) of the strains presented the phenotypic profile for ESBL production. The isolates showed positivity to at least 13.64% (03/22) of the genes studied and the highest frequencies were observed in genes sul1 (73%), dfrA12 (55%), blaCTX-M (55%), tetA, tetB and tetC, with 45%. In conclusion, the strains of Salmonella spp. isolates present genotypic and phenotypic characteristics for MDR and ESBL production, demonstrating the dissemination risk of these microorganisms through the food chain.(AU)

Salmonella spp. é um dos principais agentes responsáveis por infecção de origem alimentar em humanos, sendo os produtos de origem avícola apontados como as fontes de infecção mais frequentes. Estudos demonstraram a ocorrência de Salmonella spp. resistente a antimicrobianos em produtos de origem animal. As β-lactamases de espectro extendido (ESBL) são enzimas que conferem às bactérias a capacidade de hidrolisar cefalosporinas com uma cadeia lateral oximino e monobactâmicos. Este estudo objetivou investigar o perfil de resistência a antimicrobianos, identificar fenótipos e genótipos de multirresistência a drogas (MDR), e produção de ESBL em isolados de Salmonella spp. provenientes da cadeia produtiva de frangos de corte. Foram utilizadas amostras de Salmonella spp. (n=11) isoladas de aves, produtos e ambiente de origem avícola do estado do Maranhão - Brasil. Os isolados de Salmonella spp. avaliados apresentaram resistência múltipla a drogas tanto genotípica quanto fenotipicamente. Os resultados mostram que 72,72% (08/11) das cepas apresentaram perfil fenotípico de produção de ESBL. Os isolados apresentaram positividade a pelo menos 13,64% (03/22) dos genes pesquisados, sendo as maiores frequências observadas nos genes sul1 (73%), dfrA12 (55%), blaCTX-M (55%), tetA, tetB e tetC, com 45%. Conclui-se que as cepas de Salmonella spp. isoladas apresentam características genotípicas e fenotípicas de multirresistência a drogas e produção de ESBL, demonstrando o risco de disseminação destes microrganismos ao longo da cadeia alimentar.(AU)

Multidrug resistant and ESBL-producing Salmonella spp. isolated from poultry / Salmonella spp. produtora de ESBL e multirresistente a drogas isolada de frangos

Salmonella spp. is one of the main agents responsible for foodborne infection in humans, and products of poultry origin are the most common infection sources. Studies have shown the occurrence of antimicrobials resistant Salmonella spp. in animal products. The Extended Spectrum β-Lactamase (ESBL) are enzymes that confer to bacteria the ability to hydrolyze cephalosporin with an oximino side chain and monobactams. This study aimed to investigate antimicrobial resistance profile, identify phenotypes and genotypes for multiple drug resistance (MDR) and that produce ESBL from isolates of Salmonella spp. in the broiler production chain. We used samples of Salmonella spp. (n=11) isolates from poultry, poultry products and poultry-source environment from the state of Maranhão - Brazil. The isolates of Salmonella spp. assessed showed genotypical and phenotypical characteristics of MDR. The results show that 72.72% (08/11) of the strains presented the phenotypic profile for ESBL production. The isolates showed positivity to at least 13.64% (03/22) of the genes studied and the highest frequencies were observed in genes sul1 (73%), dfrA12 (55%), blaCTX-M (55%), tetA, tetB and tetC, with 45%. In conclusion, the strains of Salmonella spp. isolates present genotypic and phenotypic characteristics for MDR and ESBL production, demonstrating the dissemination risk of these microorganisms through the food chain.

Salmonella spp. é um dos principais agentes responsáveis por infecção de origem alimentar em humanos, sendo os produtos de origem avícola apontados como as fontes de infecção mais frequentes. Estudos demonstraram a ocorrência de Salmonella spp. resistente a antimicrobianos em produtos de origem animal. As β-lactamases de espectro extendido (ESBL) são enzimas que conferem às bactérias a capacidade de hidrolisar cefalosporinas com uma cadeia lateral oximino e monobactâmicos. Este estudo objetivou investigar o perfil de resistência a antimicrobianos, identificar fenótipos e genótipos de multirresistência a drogas (MDR), e produção de ESBL em isolados de Salmonella spp. provenientes da cadeia produtiva de frangos de corte. Foram utilizadas amostras de Salmonella spp. (n=11) isoladas de aves, produtos e ambiente de origem avícola do estado do Maranhão - Brasil. Os isolados de Salmonella spp. avaliados apresentaram resistência múltipla a drogas tanto genotípica quanto fenotipicamente. Os resultados mostram que 72,72% (08/11) das cepas apresentaram perfil fenotípico de produção de ESBL. Os isolados apresentaram positividade a pelo menos 13,64% (03/22) dos genes pesquisados, sendo as maiores frequências observadas nos genes sul1 (73%), dfrA12 (55%), blaCTX-M (55%), tetA, tetB e tetC, com 45%. Conclui-se que as cepas de Salmonella spp. isoladas apresentam características genotípicas e fenotípicas de multirresistência a drogas e produção de ESBL, demonstrando o risco de disseminação destes microrganismos ao longo da cadeia alimentar.